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Mem Inst Oswaldo Cruz, Rio de Janeiro, Vol. 104(1): 33-36, February 2009
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Prostatic paracoccidioidomycosis: differential diagnosis
of prostate cancer
Daniel Lima Lopes1, Stanley de Almeida Araújo2/+, João Paulo Lemos da Silveira Santos2,
Ana Claudia Lyon2, Diogo Vieira Dantas2, Bernardo Sgarbi Reis3, Alfredo Miranda de Góes3,
Ênio Roberto Pietra Pedroso2
Hospital do Instituto de Previdência dos Servidores do Estado de Minas Gerais, Belo Horizonte, MG, Brasil 3Departamento de
Bioquímica e Imunologia, Instituto de Ciências Biológicas 2Faculdade de Medicina, Universidade Federal de Minas Gerais,
Belo Horizonte, MG, Brasil
1
Symptomatic prostatic paracoccidioidomycosis (PCM) is a very rare condition; however, it may express as a
typical benign prostatic hyperplasia or a simulating prostatic adenocarcinoma. This case report presents PCM
mimicking prostatic adenocarcinoma. The purpose of this paper is to call the general physician’s attention to this
important differential diagnosis.
Key words: Paracoccidioides brasiliensis - paracoccidioidomycosis - prostatitis - prostate cancer
Paracoccidioidomycosis (PCM) is an important deep
mycosis in Latin America. It is caused by the dimorphic
fungus Paracoccidioides brasiliensis, whose spores enter
the body via the respiratory tract and evolve either asymptomatically or in a sub-acute or chronic manner. The parasite is able to provoke several clinical presentations due to
its capacity to disseminate itself from the lungs through
the lymphatic system or via the blood stream to any organ
or system. PCM mainly affects adult males, preferentially
in the lungs, mucosa, skin and phagocytic-monocytic system (Paniago et al. 2003, Prado et al. 2005). On a smaller
scale, it reaches the nervous, musculoskeletal and suprarenal systems (Paniago et al. 2003). Its clinical incidence
in the urinary tract, especially in prostatic injuries, is not
well known. In a few necropsy studies involving disseminated PCM cases, its incidence varies from 2.7-9% (Salfelder et al. 1969, Begliomini et al. 1993).
Prostatic diseases have become more common due to
the increase in the population’s age. Generally, they appear
in males over 40-years-old, being more often bacterial and
viral infections, benign hyperplasia and adenocarcinoma.
Prostatic adenocarcinoma is the most fearful lesion due to
its malignant and metastatic potential, and it is seen clinically in 10% of cases. Its diagnosis must always be set
apart because its mortality is 3%, making it the greatest
cause of morbi-mortality among men (Crawford 2003).
Fungal prostatitis is unusual, having as its most common agents Coccidioides immitis, Candida albicans,
Aspergillus sp., Cryptococcus neoformans and Blastomyces dermatitidis, which mainly affect patients who
are immune-suppressed. The symptomatic attack of the
prostate by PCM has rarely been described. Its potential
severity justifies the reporting of this case.
+ Corresponding autor: [email protected]
Received 3 September 2008
Accepted 21 January 2009
In this paper, infection of the prostate by P. brasiliensis is described, mimicking cancer with urethral obstruction and urgent expansion of the bladder.
Case study
AAF, a 54-year-old married rural worker who was
born in and is a current resident of São Sebastião do Maranhão, Minas Gerais, Brazil, presented in December
2003 with palate stomatitis associated with dysphagia
and odynophagia. A biopsy of this injury revealed P.
brasiliensis. He was treated with Sulfametoxazol (800
mg) and Trimethoprim (160 mg) daily in an irregular
way for 20 months. In December 2004, he started to
complain of dysuria, polyuria and urinary urgency and
frequency, which culminated after one year in prompt
urinary retention. Concomitantly, a stomatitis with
moriforme injury of the palate appeared.
A digital rectal exam revealed an increased prostate
volume, induration, precise limits and a nodule on the
right lobe. It was thought to be prostate cancer. His PSA
level was measured at 0.563 ng/mL and transrectal ultrasonography demonstrated a prostrate with irregular
contours, with peripheral zones containing hypoechoic
areas with heterogenic texture (Fig. 1). There was a volumetric increasing of the gland, which weighed 57.9 g.
The prostatic biopsy revealed a diffuse chronic granulomatous inflammatory process showing epithelial and
multinucleated giant cells, neutrophils and eosinophils
involving the P. brasiliensis (Fig. 2 A, B).
A complete blood count showed a total counting of
leukocytes of 12,940/mm3 (neutrophils 9,614/mm3, lymphocyte 2,057/mm3, eosinophils 349/mm3, basophils 116/
mm3, monocytes 660/mm3). The urine exam revealed
hemoglobin +/4+, urobilinogen 0.2 mg/dL, leukocytes
+/4+, piocytes 20/field, red blood cells 10/field, bacterian
microbiota +++/4+, rare grouped piocytes and the presence of renal epithelium. Gram staining did not reveal
any bacteria and serum biochemistry did not show any
abnormalities. A chest X-ray showed localized micro-reonline | memorias.ioc.fiocruz.br
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Prostatic paracoccidioidomycosis • Daniel Lima Lopes et al.
ticulo-nodule alterations, mainly on the hilum and in the
pulmonar basis bilaterally. Abdominal ultrasonography
did not show any alteration and the other urinary organs
were apparently normal.
Collected blood samples were positive in anti-P. brasiliensis serologic tests using the antigens PB28, Pbgp43 and
membrane and extracellular antigens (MEXO) (Fig. 3).
The initial treatment was done with Itraconazol (100
mg per day), which was replaced after 10 days with Sulfametoxazol (800 mg) and Trimetoprim (160 mg every
12 h) because the former was not available at public
health care centres in Brazil. After six months, the patient was asymptomatic and without deficits or clinical
or radiological residual injuries. The total PSA level remained low despite the intense inflammation (Fig. 4).
After one year of ambulatory observation, there
was no recurrence of the infection or side effects from
the treatment.
Fig. 1: prostatic transrectal ultra-sound. Prostate with regular contours
and precise borders. The peripheric zones present hypoechoic areas
with heterogenic textures. Prostrate mesures: longitudinal: 57.0 mm;
anti-posterior: 39.6 mm; transverse: 46.6 mm; prostatic weigh: 57.9 g.
Data compatible with the general volumetric increasing of the prostate.
Fig. 3: serum tested by enzyme-linked immunosorbent assays results
for the extracelular antigens and membranes, PB28 and Pbgp43, made
in the acute fase of patient’s disease.
Fig. 4: total prostatic-specific antigen (PSA) serum variation after one
year of medical following.
DISCUSSION
Fig. 2: biopsy by thin needle of prostatic tissue. A (Grocott): many
yeasts in the tissue. In detail, yeast with multiple sprouting (400X):
B (HE): chronical granulomatosis inflamatory process, epitheliodcells and multinucleus giant cells involving parasites (100X).
We report this case due to the rare presentation of
PCM in the prostate, which may be a serious symptomatic condition if untreated and due to the importance of
the differential diagnosis with prostate adenocarcinoma,
which is a very severe disease, with lethality and me-
Mem Inst Oswaldo Cruz, Rio de Janeiro, Vol. 104(1), February 2009
tastatic potential whose possibility of treatment is only
surgical. Depending on the extension of the neoplastic
tissue and on the chosen technique, prostatectomy may
lead to minor or serious complications such as erectile
problems urinary incontinence and damage to the urethra or rectum (Wilt & Brawer 1999). Thus, a proper
histopathological exam may demonstrate an infectious
prostatitis and avoid an unnecessary surgical intervention and its related risks.
PCM has special importance in Latin America, where
it is endemic among infecto-parasitarian diseases due to
the severity and the peculiarity of some of its clinical
forms. This infection is not commonly isolated in the
urogenital tract. PCM in the prostate is not considered
a primary disease, affecting only 1.59% of patients in
the disseminated form (Brito & Caprini 1959, Ciconelli
et al. 1969, Begliomini et al. 1993). All of the urogenital tract may be affected by the disease, including the
epididymis, testicles, prostate, ureters, penis, urethra
and kidneys. The first case of prostatic involvement was
described by Brito and Caprini (1959); since then, only
a few other cases have been described (Melo et al. 1992,
Severo et al. 2000).
Because of the general symptoms, the diagnosis of
PCM is frequently done later than expected. Patients
with prostatic involvement may present obstruction
symptoms of the lower urinary tract.
Cancer and chronic inflammation always constitute
the differential diagnosis for complaints related to prostatic disease symptoms.
When the prostate is involved in PCM infection,
differential diagnosis with cancer is difficult due to
the variety of damage and absence of specific signs.
The diagnosis of prostatic injuries is suggested by the
clinical aspects, but it often requires confirmation by a
histopathological exam. A biopsy is mandatory due to
the necessity for cancer exclusion (Stillwell et al. 1987).
Differential diagnosis for PCM of the prostate is divided
into specific, caused by bacteria (Treponema pallidum,
Mycobacterium tuberculosis, Brucella sp.), fungi (Candida sp., Aspergillus sp., C. neoformans, Histoplasma
capsulatum, Actinomyces sp., B. dermatitidis and C.
immitis), viruses or parasites, and non-specific, derived
from xantogranulomatousis, allergies, post-TURP or
post-biopsies.
Granulomatous prostatitis is a rare disease that frequently simulates the development of prostatic carcinoma
due to the formation of nodules and the increase of the
gland by rectal touch (Stillwell et al. 1987, Begliomini
et al. 1993). A histopathological exam of the granulomatous prostatitis, however, showed infiltrated lymphoplasmocyte, pseudotubercules, epithelioidic cells and
the absence of signs of atypical cellular proliferation,
which characterize the neoplasia. In coccidioidomicosis and North American blastomicosis, the involvement
of the genitourinary tract is frequent, being common in
prostatic attack in the disseminated form (Brito &
Caprini 1959, Stewart 1964, Eickenberg et al. 1975).
There have been a few cases of transmission of B. dermatitidis from men with prostatic involvement to their
female sexual partner (Faber et al. 1968). PCM has no
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record of inter-human transmission despite its potential
for sexual transfer by contaminated prostatic secretion.
Tuberculosis or other mycotic diseases that affect
the genitourinary tract are other important differential
diagnoses and the microbiologic study of urine and cultures are fundamental for its discernment (Stillwell et
al. 1987). Since P. brasiliensis is not coloured by Gram
stain, its diagnosis may not be noticed in routine exams.
Induration of the prostate may persist upon physical examination for years and scarring and fibrosis have
been observed in a third of the patients (Paniago et al.
2003). The case described here presented sexual dysfunction after the treatment and the effects tobacco use,
aging process and adverse effect of the treatment with
Sulfametoxazol-Trimetoprim or Ketoconazole, which
were concomitant conditions in this case, could be potential factors, in addition to prostate fibrosis induced by
PCM (Brito & Carpini 1959).
There is no report of alterations in serum levels of
the prostatic-specific antigen PSA during the treatment.
In granulomatous prostatitis, both increasing and decreasing serum levels of PSA may be observed. A significant reduction in PSA, as in this case, suggests that
cytokines derived from the activated macrophages and
T-lymphocytes may have a regulatory effect on the cells’
secretions and cause the destruction of the prostatic epithelia (Dhundee & Maciver 1991).
Current serum tests are highly sensitive and specific
for diagnosis and useful for the clinical follow-up of people
affected with PCM. Normal serum results are extremely
rare with evidence of the disease’s histopathology.
Serum tested by enzyme-linked immunosorbent assays (ELISA) for the extracellular antigens and membranes - MEXO - from P. brasiliensis presents a specificity of 96.6% compared to control groups and 81.2%
in relation to groups with diverse infections (Reis et al.
2005). A purified protein with a molecular weight of
28-kDa of MEXO, called Pb28, is the most specific antigen in the humoral immunological response of PCM.
This protein reacts and has a specificity of 100%. It may
be used as an alternative antigen to the serum diagnostic method. ELISA, either for MEXO or for Pb28, is a
strong reactor in serum analysis when collected during
the acute period of the disease (Fig. 4). However, one
glycoprotein with a molecular weight of 43 Kda, known
as Pbgp43, which is an important extracellular component released by P. brasiliensis during its pathogenic
phase, is used in the detection of the serum antibodies in
patients with PCM and in epidemiologic studies through
the intradermal reaction (Kalmar et al. 2004). It presents
a sensitivity of 95.1% and a specificity of 97.5%. In this
case, it was reactor-moderated (Fig. 4).
Such serum data is in accordance with those reported
by Reis et al. (2005) because Pb28 has proven to be more
sensitive and specific for PCM and Pbgp43 presented irregular results.
PCM is diagnosed by the identification of the yeasts
in direct exams of clinical samples (biopsy, mucous,
scratched) or cultures. The yeast has specific microscopic
aspects, including a bi-refringent wall, reproduction by
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Prostatic paracoccidioidomycosis • Daniel Lima Lopes et al.
multiple-sprouting and originating blastospores that do
not detach from the mother cell, which gives them a unique
appearance among the pathogenic fungi (Fig. 2A).
The granuloma is formed with the objective of restricting the parasite and avoiding its dissemination (Fig.
2B). Thus, the more efficient the cellular immunologic
response is the better the efficiency of the granulomatos reaction and the lesser the severity of the disease.
The histopathological response of the host caused by P.
brasiliensis resembles tissue invasion by B. dermatitidis
and C. immitis.
Injuries of the oropharyngeal mucosa are frequently
observed. The most characteristic aspect is moriform ulcerous stomatitis.
PCM is a disease that lacks standards for cure and a
standard treatment protocol. There are no specific treatments for the urogenital form. Prolonged medication is,
in many cases, necessary to prevent recurrence, which
exhausts the patient and impairs his/her adequate compliance with the proposed treatment. Interruption of the
medication or irregular or inadequate use may drive the
emergence of resistance, making the problem worse and
producing several side-effects (Prado et al. 2005).
Once a diagnosis of prostatic PCM is made, a specialist in infectious diseases should be consulted. Finally,
the patient needs to be observed for many years for prevention and occasional treatment of disease recurrence.
PCM is a systemic disease with the potential for involvement of all organs and it is necessary to pay attention to all complaints presented by the patients, even
those not associated with the most frequent localizations
of the disease. In South America, especially in Brazil,
prostatic PCM is an important differential diagnosis to
prostatic adenocarcinoma and can evolve into a serious
symptomatic condition if left untreated.
REFERENCES
Crawford ED 2003. Epidemiology of prostate cancer. Urology 62:
3-12.
Dhundee J, Maciver AG 1991. An immunohistological study of granulomatous prostatitis. Histopathology 18: 435-441.
Eickenberg H-U, Amin M, Lich R Jr 1975. Blastomycosis of the genitourinary tract. J Urol 113: 650-652.
Faber ER, Leahy MS, Meadows TR 1968. Endometrial blastomycosis
acquired by sexual contact. Obst Gynec 32: 195-199.
Kalmar EM, Alencar FE, Alves FP, Pang LW, Del Negro GM, Camargo
ZP, Shikanai-Yasuda MA 2004. Paracoccidioidomycosis: an epidemiologic survey in a pediatric population from the Brazilian
Amazon using skin tests. Am J Trop Med Hyg 71: 82-86.
Melo CR, Melo IS, Cerski CT 1992. Leukaemic infiltration, paracoccidioidomycosis and nodular hyperplasia of the prostate.
Br J Urol 70: 329-330.
Paniago AM, Aguiar JI, Aguiar ES, da Cunha RV, Pereira GR, Londero AT, Wanke B 2003. Paracoccidioidomycosis: a clinical and
epidemiological study of 422 cases observed in Mato Grosso do
Sul. Rev Soc Bras Med Trop 36: 455-459.
Prado FL, Prado R, Gontijo CC, Freitas RM, Pereira MC, Paula IB,
Pedroso ER 2005. Lymphoabdominal paracoccidioidomycosis
simulating primary neoplasia of the biliary tract. Mycopathologia 160: 25-28.
Reis BS, Bozzi A, Prado FL, Pereira MC, Ferreira FE, Godoy P, Moro
L, Pedroso EP, Leite MF, Goes AM 2005. Membrane and extracellular antigens of Paracoccidioides brasiliensis (Mexo): identification of a 28-kDa protein suitable for immunodiagnosis of
paracoccidioidomycosis. J Immunol Methods 307: 118-126.
Salfelder K, Doehnert G, Doehnert HR 1969. Paracoccidioidomycosis. Anatomic study with complete autopsies. Virchows Arch A
Pathol Pathol Anat 348: 51-76.
Severo LC, Kauer CL, Oliveira F, Rigatti RA, Hartmann AA, Londero AT 2000. Paracoccidioidomycosis of the male genital tract.
Report of eleven cases and a review of Brazilian literature. Rev
Inst Med Trop Sao Paulo 42: 38-40.
Begliomini H, Gorga CFA, França LCM 1993. Paracoccidioidomicose prostática. Relato de caso e revisão da literatura. J Bras Urol
19: 285-288.
Stewart BG 1964. Epididymitis and prostatitis due to coccidioidomycosis: a case report with 5-year followup. J Urol 91: 280-281.
Brito RR, Caprini N 1959. Blastomicose da próstata. Rev Paul Med
54: 116-122.
Stillwell TJ, Engen DE, Farrow GM 1987. The clinical spectrum of granulomatous prostatitis: a report of 200 cases. J Urol 138: 320-323.
Ciconelli AJ, Martins ACP, Costa RB, Fioranai SAS 1969. Blastomicose Prostática. Rev Bras Cirurg 57: 208-11.
Wilt TJ, Brawer MK 1999. Clinical evidence: non-metastatic prostate
cancer. West J Med 171: 97-101.